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DOID:0111524 - autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5
Disease Ontology Definition:A chronic progressive external ophthalmoplegia that has_material_basis_in homozygous or compound heterozygous mutation in the TOP3A gene on chromosome 17p11.2.
Synonyms: PEOB5, autosomal recessive progressive external ophthalmoplegia 5,
Xenbase Genes : top3a
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee